Organocatalytic Formal Intramolecular [3+2]-Cycloaddition to Acquire Biologically Important Methanodibenzo[a,f]azulenes and Methanobenzo[f]azulenes

dc.contributor.author	Peraka, Swamy
dc.contributor.author	Pasha, Mohammed Anif
dc.contributor.author	Thirupathi, Guguloth
dc.contributor.author	Ramachary, Dhevalapally B.
dc.date.accessioned	2022-03-27T09:37:07Z
dc.date.available	2022-03-27T09:37:07Z
dc.date.issued	2019-11-07
dc.description.abstract	Lawsones were transformed into the functionally rich framework of methanodibenzo[a,f]azulenes and methanobenzo[f]azulenes in a single- or two-pot operation through five organocatalytic sequential reactions in very good yields with excellent selectivities. These resultant molecules are basic skeletons of important antibiotics, which highlights the value of this formal intramolecular [3+2]-cycloaddition as a key protocol.
dc.identifier.citation	Chemistry - A European Journal. v.25(62)
dc.identifier.issn	09476539
dc.identifier.uri	10.1002/chem.201902453
dc.identifier.uri	https://onlinelibrary.wiley.com/doi/10.1002/chem.201902453
dc.identifier.uri	https://dspace.uohyd.ac.in/handle/1/13120
dc.subject	Knoevenagel condensation
dc.subject	lawsones
dc.subject	methanobenzo[f]azulenes
dc.subject	organocatalysis
dc.subject	[3+2]-cycloaddition
dc.title	Organocatalytic Formal Intramolecular [3+2]-Cycloaddition to Acquire Biologically Important Methanodibenzo[a,f]azulenes and Methanobenzo[f]azulenes
dc.type	Journal. Article
dspace.entity.type

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